A Convenient Synthesis of 3-Aryl-2-Methyl-3,4-Dihydro-1(2H)-Isoquinolones and -1,2,3,4-Tetrahydroisoquinolines
摘要:
A new methodology for the synthesis of 3-aryl-2-methyl-3,4-dihydro-2H-isoquinolin-1-ones and 3-aryl-2-methyl-1,2,3,4-tetrahydroisoquinolines is reported.
Fluoride ion-induced cyclization of o-[bis(trimethylsilyl)methyl]-N-acylbenzamide derivatives. New efficient synthesis of 2,3-differentially substituted 1(2H)-isoquinolones
DYKE S. F.; THORNS J. F.; HEDGES S. H.; WIGGINS D. W., TETRAHEDRON, 1979, 35, NO 15, 1861-1867
作者:DYKE S. F.、 THORNS J. F.、 HEDGES S. H.、 WIGGINS D. W.
DOI:——
日期:——
Fluoride ion-induced cyclization of o-[bis(trimethylsilyl)methyl]-N-acylbenzamide derivatives. New efficient synthesis of 2,3-differentially substituted 1(2H)-isoquinolones
A wide variety of 2-alkyl-3-alkyl, -3-aryl and
-3-heteroaryl-1(2H)-isoquinolones have been obtained
by fluoride ion-induced intramolecular alkenation of
o-[bis(trimethylsilyl)methyl]-N
-acylbenzamide derivatives.
A new methodology for the synthesis of 3-aryl-2-methyl-3,4-dihydro-2H-isoquinolin-1-ones and 3-aryl-2-methyl-1,2,3,4-tetrahydroisoquinolines is reported.